• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Prognostic significance of Bcl-6 protein expression in DLBCL treated with CHOP or R-CHOP: a prospective correlative study.CHOP或R-CHOP治疗的弥漫性大B细胞淋巴瘤中Bcl-6蛋白表达的预后意义:一项前瞻性相关性研究。
Blood. 2006 Jun 1;107(11):4207-13. doi: 10.1182/blood-2005-10-4222. Epub 2006 Jan 31.
2
Rituximab plus CHOP (R-CHOP) overcomes bcl-2--associated resistance to chemotherapy in elderly patients with diffuse large B-cell lymphoma (DLBCL).利妥昔单抗联合环磷酰胺、阿霉素、长春新碱和泼尼松(R-CHOP)方案克服了弥漫性大B细胞淋巴瘤(DLBCL)老年患者中与bcl-2相关的化疗耐药性。
Blood. 2003 Jun 1;101(11):4279-84. doi: 10.1182/blood-2002-11-3442. Epub 2003 Feb 6.
3
Prognostic impact of immunohistochemical biomarkers in diffuse large B-cell lymphoma in the rituximab era.利妥昔单抗时代免疫组化生物标志物对弥漫性大B细胞淋巴瘤的预后影响
Cancer Sci. 2009 Oct;100(10):1842-7. doi: 10.1111/j.1349-7006.2009.01268.x. Epub 2009 Jul 1.
4
BCL2 positive and BCL6 negative diffuse large B cell lymphoma patients benefit from R-CHOP therapy irrespective of germinal and non germinal center B cell like subtypes.BCL2阳性且BCL6阴性的弥漫性大B细胞淋巴瘤患者,无论其为生发中心B细胞样亚型还是非生发中心B细胞样亚型,均可从R-CHOP治疗中获益。
J BUON. 2015 May-Jun;20(3):820-8.
5
Expression of p21 protein predicts clinical outcome in DLBCL patients older than 60 years treated with R-CHOP but not CHOP: a prospective ECOG and Southwest Oncology Group correlative study on E4494.p21蛋白的表达可预测接受R-CHOP而非CHOP治疗的60岁以上弥漫性大B细胞淋巴瘤(DLBCL)患者的临床结局:一项针对E4494的前瞻性东部肿瘤协作组(ECOG)和西南肿瘤协作组相关性研究。
Clin Cancer Res. 2010 Apr 15;16(8):2435-42. doi: 10.1158/1078-0432.CCR-09-1219. Epub 2010 Apr 6.
6
Rituximab-CHOP versus CHOP alone or with maintenance rituximab in older patients with diffuse large B-cell lymphoma.利妥昔单抗联合CHOP方案与单纯CHOP方案或CHOP方案联合利妥昔单抗维持治疗老年弥漫性大B细胞淋巴瘤的比较。
J Clin Oncol. 2006 Jul 1;24(19):3121-7. doi: 10.1200/JCO.2005.05.1003. Epub 2006 Jun 5.
7
CHOP-R therapy overcomes the adverse prognostic influence of BCL-2 expression in diffuse large B-cell lymphoma.CHOP-R疗法克服了弥漫性大B细胞淋巴瘤中BCL-2表达的不良预后影响。
Leuk Lymphoma. 2007 Jun;48(6):1102-9. doi: 10.1080/10428190701344881.
8
Short-term efficacy of rituximab-CHOP and CHOP regimens on two subtypes of diffuse large B-cell lymphoma.利妥昔单抗-CHOP方案与CHOP方案对两种弥漫性大B细胞淋巴瘤亚型的短期疗效。
Ai Zheng. 2009 Feb;28(2):146-9. Epub 2009 Feb 15.
9
Outcome of elderly patients with diffuse large B-cell lymphoma treated with R-CHOP: results from the UK NCRI R-CHOP14v21 trial with combined analysis of molecular characteristics with the DSHNHL RICOVER-60 trial.接受R-CHOP治疗的老年弥漫性大B细胞淋巴瘤患者的结局:来自英国国家癌症研究所R-CHOP14v21试验以及与DSHNHL RICOVER-60试验分子特征联合分析的结果。
Ann Oncol. 2017 Jul 1;28(7):1540-1546. doi: 10.1093/annonc/mdx128.
10
Clinical Impact of the Cell-of-Origin Classification and the MYC/ BCL2 Dual Expresser Status in Diffuse Large B-Cell Lymphoma Treated Within Prospective Clinical Trials of the German High-Grade Non-Hodgkin's Lymphoma Study Group.在德国高级非霍奇金淋巴瘤研究组的前瞻性临床试验中,针对弥漫性大 B 细胞淋巴瘤进行治疗,探讨了细胞起源分类和 MYC/BCL2 双表达状态的临床影响。
J Clin Oncol. 2017 Aug 1;35(22):2515-2526. doi: 10.1200/JCO.2016.70.3660. Epub 2017 May 19.

引用本文的文献

1
Bibliometric analysis and visualization of global research trends in primary thyroid lymphoma via CiteSpace.通过CiteSpace对原发性甲状腺淋巴瘤全球研究趋势进行文献计量分析和可视化
Gland Surg. 2024 Nov 30;13(11):2078-2097. doi: 10.21037/gs-24-317. Epub 2024 Nov 26.
2
Advances in biology, diagnosis and treatment of DLBCL.弥漫性大 B 细胞淋巴瘤的生物学、诊断和治疗进展。
Ann Hematol. 2024 Sep;103(9):3315-3334. doi: 10.1007/s00277-024-05880-z. Epub 2024 Jul 17.
3
The F-box E3 ligase protein FBXO11 regulates EBNA3C-associated degradation of BCL6.F-box E3 连接酶蛋白 FBXO11 调控 EBNA3C 相关的 BCL6 降解。
J Virol. 2024 Jul 23;98(7):e0054824. doi: 10.1128/jvi.00548-24. Epub 2024 Jun 12.
4
Clinicopathological analysis of diffuse large B-cell lymphoma using molecular biomarkers: a retrospective analysis from 7 Hungarian centers.使用分子生物标志物对弥漫性大B细胞淋巴瘤进行临床病理分析:来自7个匈牙利中心的回顾性分析
Front Oncol. 2023 Sep 8;13:1224733. doi: 10.3389/fonc.2023.1224733. eCollection 2023.
5
Potential Prognostic and Predictive Role of Monocyte and Lymphocyte Counts on Presentation in Patients Diagnosed With Diffuse Large B-Cell Lymphoma.单核细胞和淋巴细胞计数对初诊弥漫性大B细胞淋巴瘤患者的潜在预后及预测作用
Cureus. 2023 Mar 1;15(3):e35654. doi: 10.7759/cureus.35654. eCollection 2023 Mar.
6
MUM1 Expression versus Hans Algorithm to Predict Prognosis in Indonesian Diffuse Large B-Cell Lymphoma Patients Receiving R-CHOP.MUM1表达与汉斯算法在预测接受R-CHOP治疗的印度尼西亚弥漫性大B细胞淋巴瘤患者预后中的比较
Cancer Manag Res. 2022 Mar 1;14:925-935. doi: 10.2147/CMAR.S345745. eCollection 2022.
7
Development and validation of prognostic scoring in primary intestinal diffuse large B-cell lymphoma: a single-institution study of 184 patients.原发性肠道弥漫性大B细胞淋巴瘤预后评分系统的开发与验证:一项针对184例患者的单机构研究
Ann Transl Med. 2021 Oct;9(20):1542. doi: 10.21037/atm-21-4761.
8
Prognostic molecular biomarkers in diffuse large B-cell lymphoma in the rituximab era and their therapeutic implications.利妥昔单抗时代弥漫性大B细胞淋巴瘤的预后分子生物标志物及其治疗意义。
Ther Adv Hematol. 2021 May 24;12:20406207211013987. doi: 10.1177/20406207211013987. eCollection 2021.
9
Rituximab-Based Therapy in Newly Diagnosed Diffuse Large B-Cell Lymphoma Patients: Individualized Risk-Adapted Therapy Approach Using Molecular Subtypes.基于利妥昔单抗的疗法用于新诊断的弥漫性大B细胞淋巴瘤患者:采用分子亚型的个体化风险适应性治疗方法
J Hematol. 2017 Sep;6(2-3):33-43. doi: 10.14740/jh320w. Epub 2017 Jul 20.
10
Role of radiation therapy in primary breast diffuse large B-cell lymphoma in the Rituximab era: a SEER database analysis.放疗在利妥昔单抗时代原发性乳腺弥漫性大 B 细胞淋巴瘤中的作用:SEER 数据库分析。
Cancer Med. 2018 May;7(5):1845-1851. doi: 10.1002/cam4.1457. Epub 2018 Apr 6.

本文引用的文献

1
BCL6 interacts with the transcription factor Miz-1 to suppress the cyclin-dependent kinase inhibitor p21 and cell cycle arrest in germinal center B cells.BCL6与转录因子Miz-1相互作用,以抑制生发中心B细胞中的细胞周期蛋白依赖性激酶抑制剂p21并阻止细胞周期。
Nat Immunol. 2005 Oct;6(10):1054-60. doi: 10.1038/ni1245. Epub 2005 Sep 4.
2
Deregulated BCL6 expression recapitulates the pathogenesis of human diffuse large B cell lymphomas in mice.BCL6表达失调在小鼠中重现了人类弥漫性大B细胞淋巴瘤的发病机制。
Cancer Cell. 2005 May;7(5):445-55. doi: 10.1016/j.ccr.2005.03.037.
3
Small molecule inhibitors of IkappaB kinase are selectively toxic for subgroups of diffuse large B-cell lymphoma defined by gene expression profiling.IkappaB激酶的小分子抑制剂对通过基因表达谱定义的弥漫性大B细胞淋巴瘤亚组具有选择性毒性。
Clin Cancer Res. 2005 Jan 1;11(1):28-40.
4
Rituximab (chimeric anti-CD20 monoclonal antibody) inhibits the constitutive nuclear factor-{kappa}B signaling pathway in non-Hodgkin's lymphoma B-cell lines: role in sensitization to chemotherapeutic drug-induced apoptosis.利妥昔单抗(嵌合抗CD20单克隆抗体)抑制非霍奇金淋巴瘤B细胞系中组成型核因子-κB信号通路:在化疗药物诱导的细胞凋亡致敏中的作用。
Cancer Res. 2005 Jan 1;65(1):264-76.
5
The BCL6 proto-oncogene suppresses p53 expression in germinal-centre B cells.BCL6原癌基因抑制生发中心B细胞中的p53表达。
Nature. 2004 Dec 2;432(7017):635-9. doi: 10.1038/nature03147.
6
Molecular profiling of diffuse large B-cell lymphoma identifies robust subtypes including one characterized by host inflammatory response.弥漫性大B细胞淋巴瘤的分子谱分析确定了多种明确的亚型,其中一种以宿主炎症反应为特征。
Blood. 2005 Mar 1;105(5):1851-61. doi: 10.1182/blood-2004-07-2947. Epub 2004 Nov 18.
7
Specific peptide interference reveals BCL6 transcriptional and oncogenic mechanisms in B-cell lymphoma cells.特异性肽干扰揭示B细胞淋巴瘤细胞中BCL6的转录和致癌机制。
Nat Med. 2004 Dec;10(12):1329-35. doi: 10.1038/nm1134. Epub 2004 Nov 7.
8
Inhibition of the Raf-MEK1/2-ERK1/2 signaling pathway, Bcl-xL down-regulation, and chemosensitization of non-Hodgkin's lymphoma B cells by Rituximab.利妥昔单抗对Raf-MEK1/2-ERK1/2信号通路的抑制、Bcl-xL的下调以及非霍奇金淋巴瘤B细胞的化学增敏作用。
Cancer Res. 2004 Oct 1;64(19):7117-26. doi: 10.1158/0008-5472.CAN-03-3500.
9
From the bench to the bedside: ways to improve rituximab efficacy.从实验室到临床:提高利妥昔单抗疗效的方法。
Blood. 2004 Nov 1;104(9):2635-42. doi: 10.1182/blood-2004-03-1110. Epub 2004 Jun 29.
10
Prediction of survival in diffuse large-B-cell lymphoma based on the expression of six genes.基于六个基因的表达对弥漫性大B细胞淋巴瘤生存情况的预测
N Engl J Med. 2004 Apr 29;350(18):1828-37. doi: 10.1056/NEJMoa032520.

CHOP或R-CHOP治疗的弥漫性大B细胞淋巴瘤中Bcl-6蛋白表达的预后意义:一项前瞻性相关性研究。

Prognostic significance of Bcl-6 protein expression in DLBCL treated with CHOP or R-CHOP: a prospective correlative study.

作者信息

Winter Jane N, Weller Edie A, Horning Sandra J, Krajewska Maryla, Variakojis Daina, Habermann Thomas M, Fisher Richard I, Kurtin Paul J, Macon William R, Chhanabhai Mukesh, Felgar Raymond E, Hsi Eric D, Medeiros L Jeffrey, Weick James K, Reed John C, Gascoyne Randy D

机构信息

Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.

出版信息

Blood. 2006 Jun 1;107(11):4207-13. doi: 10.1182/blood-2005-10-4222. Epub 2006 Jan 31.

DOI:10.1182/blood-2005-10-4222
PMID:16449523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1895783/
Abstract

Bcl-6 protein expression, a marker of germinal center origin, has been associated with a favorable prognosis in diffuse large B-cell lymphoma (DLBCL). To determine the prognostic significance of this marker when rituximab (R) was added to cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy, we prospectively studied Bcl-6 protein expression by immunohistochemical staining of 199 paraffin-embedded specimens from patients enrolled in the US Intergroup phase 3 trial comparing R-CHOP to CHOP with or without maintenance R. In Bcl-6(-) patients, failure-free survival (FFS) and overall survival (OS) were prolonged for those treated with R-CHOP alone compared to CHOP alone (2-year FFS 76% versus 9%, P < .001; 2-year OS 79% versus 17%, P < .001). In contrast, no differences in FFS and OS were detected between treatment arms for Bcl-6(+) cases. In the multivariate analysis, treatment arm (CHOP versus R-CHOP) was the major determinant of both FFS (P < .001) and OS (P < .001) for the Bcl-6(-) subset, whereas the International Prognostic Index risk group was the only significant predictor of outcome among Bcl-6(+) cases. Bcl-2 protein expression was not predictive of outcome in either group. In this study, we observed a reduction in treatment failures and death with the addition of R to CHOP in Bcl-6(-) DLBCL cases only. Our finding that Bcl-6(+) cases did not benefit from the addition of R to CHOP requires independent confirmation.

摘要

生发中心起源的标志物Bcl-6蛋白表达与弥漫性大B细胞淋巴瘤(DLBCL)的良好预后相关。为了确定在环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)化疗中加入利妥昔单抗(R)时该标志物的预后意义,我们通过免疫组织化学染色对199例石蜡包埋标本进行了前瞻性研究,这些标本来自参与美国协作组3期试验的患者,该试验比较了R-CHOP与CHOP(加或不加维持性R)。在Bcl-6(-)患者中,与单纯CHOP治疗相比,单纯R-CHOP治疗的无失败生存期(FFS)和总生存期(OS)延长(2年FFS 76%对9%,P<0.001;2年OS 79%对17%,P<0.001)。相比之下,Bcl-6(+)病例的各治疗组之间在FFS和OS方面未检测到差异。在多变量分析中,治疗组(CHOP与R-CHOP)是Bcl-6(-)亚组FFS(P<0.001)和OS(P<0.001)的主要决定因素,而国际预后指数风险组是Bcl-6(+)病例中唯一显著的预后预测指标。Bcl-2蛋白表达在两组中均不能预测预后。在本研究中,我们仅在Bcl-6(-)DLBCL病例中观察到CHOP加用R可减少治疗失败和死亡。我们发现Bcl-6(+)病例未从CHOP加用R中获益,这一发现需要独立验证。